ITEM #352/#CS352* CONTACT LENS CASES— 510(k) K890533
Substantially EquivalentMagnivision, Inc.
FDA 510(k) clearance K890533 for ITEM #352/#CS352* CONTACT LENS CASES, Substantially Equivalent on 1989-06-23. Applicant: Magnivision, Inc.. Device class: 2.
Clearance details
- Applicant
- Magnivision, Inc.
- Product code
- Code LRX
- Device class
- Class 2
- Regulation
- 21 CFR 886.5928
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
Recent devices under product code LRX
view all- K252175 — LANDR Contact LENS Case
- K250495 — MINI VP1 (PL67_F); MINI VP1 (PL61_F)
- K240095 — CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)
- K231123 — Phoenix Contact Lens Case - dome top flat pack (CL-01) +2 more
- K173538 — Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODisc
More clearances from Magnivision, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.